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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1-[difluoro(methyl)silyl]ethyl-difluoro-methylsilane

CC([Si](F)(F)C)[Si](F)(F)C Request for Quotation
Chemical Name: 1-[difluoro(methyl)silyl]ethyl-difluoro-methylsilane
CAS Number: 170381-99-4
Product Number: AG00AM3F(AGN-PC-03GN9V)
Synonyms:
MDL No: MFCD03411240
Molecular Formula: C4H10F4Si2
Molecular Weight: 190.2868128

Identification/Properties

Computed Properties
Molecular Weight:
190.288g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
190.026g/mol
Monoisotopic Mass:
190.026g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
99.8
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Silane, 1,2-ethanediylbis[difluoromethyl- is a versatile compound widely used in chemical synthesis for its unique properties and diverse applications. This compound serves as a valuable building block in organic chemistry, particularly in the synthesis of complex molecules and polymers. Its di-fluoromethyl functional groups make it a valuable reagent for introducing fluorine atoms into organic molecules, which can significantly impact the properties and reactivity of the resulting products. Silane, 1,2-ethanediylbis[difluoromethyl- is utilized in various reactions such as nucleophilic substitution, cross-coupling reactions, and polymerization processes, enabling chemists to access a wide range of fluorinated compounds with tailored properties. Its use in chemical synthesis contributes to the development of new materials, pharmaceuticals, agrochemicals, and advanced technologies.